AR057983A1 - Inhibidores hterociclicos de aspartil proteasas - Google Patents
Inhibidores hterociclicos de aspartil proteasasInfo
- Publication number
- AR057983A1 AR057983A1 ARP060104660A ARP060104660A AR057983A1 AR 057983 A1 AR057983 A1 AR 057983A1 AR P060104660 A ARP060104660 A AR P060104660A AR P060104660 A ARP060104660 A AR P060104660A AR 057983 A1 AR057983 A1 AR 057983A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- arylalkyl
- aryl
- heteroaryl
- heterocycloalkyl
- Prior art date
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Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
- A61P31/18—Antivirals for RNA viruses for HIV
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
- A61P33/02—Antiprotozoals, e.g. for leishmaniasis, trichomoniasis, toxoplasmosis
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
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- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Tropical Medicine & Parasitology (AREA)
- Virology (AREA)
- Heart & Thoracic Surgery (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- AIDS & HIV (AREA)
- Cardiology (AREA)
- Molecular Biology (AREA)
- Hospice & Palliative Care (AREA)
- Psychiatry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
Se divulga el método para inhibir las aspartil proteasas, y en particular, los métodos para tratar enfermedades cardiovasculares, enfermedades cognitivas y neurodegenerativas. Además se divulgan métodos para tratar enfermedades cognitivas o neurodegenerativas utilizando los compuestos de formula (1) en combinacion con un inhibidor de colinesterasa o un agonista m1 o antagonista m2 muscarínicos. Reivindicacion 1: Un compuesto que tiene la formula estructural formula (1), o su estereoisomero, tautomero, o sal aceptable para uso farmacéutico, donde W es -S(O)-, -S(O)2-, -C(=O)-, -O-, -C(=S)-, -C(R6)(R7)-, -N(R5)-, -P(O)(OR15)- o -C(=N(R5))-; Ar es arileno o heteroarileno, donde Ar está independientemente no sustituido o sustituido con 1 a 5 grupos R14; R1, R2 y R5 se seleccionan independientemente del grupo integrado por H, alquilo, arilalquilo, heteroarilalquilo, cicloalquilalquilo, heterocicloalquilalquilo, arilcicloalquilalquilo, heteroarilcicloalquilalquilo, arilheterocicloalquilalquilo, heteroarilheterocicloalquilalquilo, cicloalquilo, ariIcicloalquilo heteroarilcicloalquilo, heterocicloalquilo, arilheterocicloalquilo, heteroarilheterocicloalquilo, alquenilo, arilalquenilo, cicloalquenilo, arilcicloalquenllo, heteroarilcicloalquenilo, heterocicloalquenilo, arilheterocicloalquenilo, heteroarilheterocicloalquenilo, alquinilo, arilalquinilo. arilo, cicloalquilarilo, heterocicloalquilarilo, heterocicloalquenilarilo, heteroarilo, cicloalquilheteroarilo, heterocicloalquilheteroarilo, cicloalquenilarilo, heterocicloalquenilarilo, -OR15, -CN, -C(O)R8, -C(O)OR9, .-S(O)R10, -S(O)2R10, -C(O)N(R11)(R12), -S(O)N(R11)(R12), -S(O)2N(R11)(R12), -NO2, -N=C(R8)2 y -N(R8)2; R3, R4, R6 y R7 se seleccionan independientemente del grupo integrado por H, alquilo, arilalquilo, heteroarilalquilo, cicloalquilalquilo, heterocicloalquilalquilo, arilcicloalquilalquilo, heteroarilcicloalquilalquilo, arilheterocicloalquilalquilo, heteroarilheterocicloalquilalquilo, cicloalquilo, arilcicloalquilo, heteroarilcicloalquilo, heterocicloalquilo, arilheterocicloalquilo, heteroarilheterocicloalquilo, alquenilo, arilalquenilo, cicloalquenilo, arilcicloalquenilo, heteroarilcicloalquenilo, heterocicloalquenilo, arilheterocicloalquenilo, heteroarilheterocicloalquenilo, alquinilo, arilalquinilo, arilo, cicloalquilarilo, heterocicloalquilarilo, heterocicloalquenilarilo, heteroarilo, cicloalquilheteroarilo, heterocicloalquilheteroarilo, cicloalquenilarilo, heterocicloalquenilarilo, -CH2-O-Si(R9)(R10)(R19), -CN, -C(O)R8, -C(O)OR9 o -C(O)N(R11)(R12); u opcionalmente, R3, R4, R6 y R7, junto con el átomo de carbono al cual están unidos forman un anillo cicloalquilo de 3 a 8 miembros opcionalmente sustituido con 1 a 4 restos R14 donde 1-5 de los átomos del anillo pueden ser reemplazados por -O-; -S-; -N(R5)-; -C(O)-; -S(O)-, o -S(O)2-; R8 se selecciona independientemente del grupo integrado por H, alquilo. alquenilo, alquinilo, cicloalquilo, cicloalquilalquilo, cicloalquenilo, heterocicloalquilo, heterocicloalquilalquilo, arilo, arilalquilo, heteroarilo, heteroarilalquilo, -OR15, -N(R15)(R16), -N(R15)C(O)R16, -N(R15)S(O)R16, -N(R15)S(O)2R16, - N(R15)S(O)2N(R16)(R17), -N(R15)S(O)N(R16)(R17), -N(R15)C(O)N(R16)(R17) y -N(R15)C(O)OR16; R9 se selecciona independientemente del grupo integrado por H, alquilo, cicloalquilo, cicloalquilalquilo, heterocicloalquilo, heterocicloalquilalquilo, arilo, arilalquilo, heteroarilo y heteroarilalquilo; R10 se selecciona independientemente del grupo integrado por H, alquilo. alquenilo, cicloalquilo, cicloalquilalquilo, cicloalquenilo, heterocicloalquilo, heterocicloalquilalquilo, arilo, arilalquilo, heteroarilo, heteroarilalquilo y -N(R15)(R16); R11 y R12 se seleccionan independientemente del grupo integrado por H, alquilo, cicloalquilo, cicloalquilalquilo, heterocicloalquilo, heterocicloalquilalquilo, arilo, arilalquilo, heteroarilo, heteroarilalquilo, -C(O)R8, -C(O)OR8, -S(O)R10, -S(O)2R10, -C(O)N(R15)(R16), -S(O)N(R15)(R16) y -S(O)2N(R15)(R16); R14 es 1-5 sustituyentes independientemente seleccionados del grupo integrado por alquilo, alquenilo, alquinilo, cicloalquilo, cicloalquilalquilo, cicloalquenilo, heterocicloalquilo, heterocicloalquilalquilo, arilo, arilalquilo, heteroarilo, heteroarilalquilo, halo, -CN, -OR15, -C(O)R15, -C(O)OR15, -C(O)N(R15)(R16), -SR15, -S(O)N(R15)(R16), -S(O)2N(R15)(R16), -C(=NOR15)R16, -P(O)(OR15)(OR16), -N(R15)(R16), -N(R15)C(O)R16, -N(R15)S(O)R16, -N(R15)S(O)2R16, -N(R15)S(O)2N(R16)(R17), -N(R15)C(O)N(R16)(R17) y -N(R15)C(O)OR16; R15, R16 y R17 se seleccionan independientemente del grupo integrado por H, alquilo, alquenilo, alquinilo, cicloalquilo, cicloalquilalquilo, heterocicloalquilo, heterocicloalquilalquilo, arilo, arilalquilo, heteroarilo, heteroarilalquilo, arilcicloalquilo, arilheterocicloalquilo, R18-alquilo, R18-cicloalquilo, R18-cicloalquilalquilo, R18- heterocicloalquilo, R18-heterocicloalquilalquilo, R18-arilo, R18-arilalquilo, R18-heteroarilo y R18-heteroarilalquilo; o R15, R16 y R17 son seleccionadas del grupo de estructuras (2), donde R23 totaliza 0 a 5 sustituyentes, m es 0 a 6 y n es 1 a 5; R18 es 1-5 sustituyentes independientemente seleccionados del grupo integrado por alquilo, alquenilo, arilo, arilalquilo, arilalquenilo, arilalquinilo, -NO2, halo, heteroarilo, HO-alquiloxialquilo, -CF3, -CN, alquil-CN, -C(O)R19, -C(O)OH, -C(O)OR19, -C(O)NHR20, -C(O)NH2, -C(O)N(alquilo)2, -C(O)N(alquil)(arilo), -C(O)N(alquil)(heteroarilo), -SR19, -S(O)2R20, -S(O)NH2, -S(O)NH(alquilo), -S(O)N(alquil)(alquilo), -S(O)NH(arilo), -S(O)2NH2, -S(O)2NHR19, -S(O)2NH(heterocicloalquilo), - S(O)2N(alquilo)2, -S(O)2N(alquil)(arilo), -OCF3, -OH, -OR20, -O-heterocicloalquilo, -O-cicloalquilalquilo, -O-heterocicloalquilalquilo, -NH2, -NHR20, -N(alquil)2, -N(arilalquilo)2, -N(arilalquil)-(heteroarilalquilo), -NHC(O)R20, -NHC(O)NH2, - NHC(O)NH(alquilo), -NHC(O)N(alquil)(alquilo), -N(alquil)C(O)NH(alquilo), -N(alquil)C(O)N(alquil)(alquilo), -NHS(O)2R20, .-NHS(O)2NH(alquilo), -NHS(O)2N(alquil)(alquilo), -N(alquil)S(O)2NH(alquilo) y -N(alquil)S(O)2N(alquil)(alquilo); o dos restos R18 sobre átomos adyacentes pueden unirse en forma conjunta para formar las estructuras del grupo de formulas (3); R19 es alquilo, cicloalquilo, arilo, arilalquilo o heteroarilalquilo; R20 es alquilo, cicloalquilo, arilo, arilo halo sustituido, arilalquilo, heteroarilo o heteroarilalquilo; y donde cada uno de los grupos alquilo, cicloalquilo, cicloalquilalquilo, heterocicloalquilo, heterocicloalquilalquilo, arilo, arilalquilo heteroarilo, heteroarilalquilo, alquenilo y alquinilo en R1, R2, R3, R4, R5, R6, R7, R8, R9, R10, R11, R12 y R14 está independientemente no sustituido o sustituido con 1 a 5 grupos R21 independientemente seleccionados del grupo integrado por alquilo, alquenilo, alquinilo, cicloalquilo, cicloalquilalquilo, cicloalquenilo, heterocicloalquilo, heterocicloalquilalquilo, arilo, arilalquilo, heteroarilo, heteroarilalquilo, halo, -CN, -OR15, -C(O)R15, -C(O)OR15, -C(O)N(R15)(R16), -SR15, -S(O)N(R15)(R16), -CH(R15)(R16), -S(O)2N(R15)(R16), -C(=NOR15)R16, - P(O)(OR15)(OR16), -N(R15)(R16), -alquil-N(R15)(R16), -N(R15)C(O)R16, -CH2-N(R15)C(O)R16, -CH2-R15; -N(R15)S(O)R16, -N(R15)S(O)2R16, -CH2-N(R15)S(O)2R16, -N(R15)S(O)2N(R16)(R17), -N(R15)S(O)N(R16)(R17), -N(R15)C(O)N(R16)(R17), -CH2- N(R15)C(O)N(R16)(R17), -N(R15)C(O)OR16, -CH2-N(R15)C(O)OR16, -S(O)R15, =NOR15, -N3, -NO2 y -S(O)2R15; y donde cada uno de los grupos alquilo, cicloalquenilo, cicloalquilo, cicloalquilalquilo, heterocicloalquilo, heterocicloalquilalquilo, arilo, arilalquilo, heteroarilo, heteroarilalquilo, alquenilo y alquinilo en R21 está independientemente no sustituido o sustituido con 1 a 5 grupos R22 independientemente seleccionados del grupo integrado por alquilo, cicloalquilo, cicloalquenilo, heterocicloalquilo, arilo, heteroarilo, halo, -CF3, -CN, -OR15, -C(O)R15, -C(O)OR15, -alquil-C(O)OR15, C(O)N(R15)(R16), -SR15, -S(O)N(R15)(R16), -S(O)2N(R15)(R16), -C(=NOR15)R16, -P(O)(OR15)(OR16), -N(R15)(R16), -alquil-N(R15)(R16), -N(R15)C(O)R16, - CH2-N(R15)C(O)R16, -N(R15)S(O)R16, -N(R15)S(O)2R16, -CH2-N(R15)S(O)2R16, -N(R15)S(O)2N(R16)(R17), -N(R15)S(O)N(R16)(R17), -N(R15)C(O)N(R16)(R17), -CH2-N(R15)C(O)N(R16)(R17), -N(R15)C(O)OR16, -CH2-N(R15)C(O)OR16, -N3, =NOR15, -NO2, -S(O)R15 y - S(O)2R15; o dos restos R21 o dos R22 sobre átomos adyacentes pueden unirse en forma conjunta para formar un resto del grupo de formulas (3); y cuando R21 o R22 se seleccionan del grupo integrado por -C(=NOR15)R16, -N(R15)C(O)R16, -CH2-N(R15)C(O)R16, -N(R15)S(O)R16, -N(R15)S(O)2N(R16)(R17), -N(R15)S(O)N(R16)(R17), -N(R15)C(O)N(R16)(R17), -CH2-N(R15)C(O)N(R16)(R17), -N(R15)C(O)OR16 y -CH2-N(R15)C(O)OR16, R15 y R16 juntos pueden ser una cadena C2 a C4 donde, opcionalmente, uno, dos o tres carbonos del anillo pueden ser reemplazados por -C(O)- o -N(H)- y R15 y R16, junto con los átomos a los cuales están unidos, forman un anillo de 5 a 7 miembros, opcionalmente sustituido con R23; R23 es 1 a 5 grupos independientemente seleccionados del grupo integrado por alquilo, alquenilo, alquinilo, cicloalquilo, cicloalquilalquilo, cicloalquenilo, heterocicloalquilo, heterocicloalquilalquilo, arilo, arilalquilo, heteroarilo, heteroarilalquilo, halo, -CN, -OR24, -C(O)R24, -C(O)OR24, -C(O)N(R24)(R25), -SR24, -S(O)N(R24)(R25), -S(O)2N(R24)(R25), -C(=NOR24)R25, -P(O)(OR24)(OR25), -N(R24)(R25), -alquil-N(R24)(R25), -N(R24)C(O)R25, -CH2-N(R24)C(O)R25, -N(R24)S(O)R25, -N(R24)S(O)2R25, -CH2-N(R24)S(O)2R25, -N(R24)S(O)2N(R25)(R26), - N(R24)S(O)N(R25)(R26), -N(R24)C(O)N(R25)(R26), -CH2-N(R24)C(O)N(R25)(R26), -N(R24)C(O)OR25, -CH2-N(R24)C(O)OR25, -S(O)R24 y -S(O)2R24 y donde cada uno de los grupos alquilo, cicloalquilo, cicloalquilalquilo, heterocicloalquilo, heterocicloalquilalquilo, arilo, arilalquilo, heteroarilo, heteroarilalquilo, alquenilo y alquinilo en R23 está independientemente no sustituido o sustituido con 1 a 5 grupos R27 independientemente seleccionados del grupo integrado por alquilo, cicloal
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US73062205P | 2005-10-27 | 2005-10-27 |
Publications (1)
Publication Number | Publication Date |
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AR057983A1 true AR057983A1 (es) | 2008-01-09 |
Family
ID=37873175
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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ARP060104660A AR057983A1 (es) | 2005-10-27 | 2006-10-25 | Inhibidores hterociclicos de aspartil proteasas |
Country Status (13)
Country | Link |
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US (3) | US7763606B2 (es) |
EP (1) | EP1940828B1 (es) |
JP (1) | JP2009513656A (es) |
CN (1) | CN101296926A (es) |
AR (1) | AR057983A1 (es) |
AT (1) | ATE478070T1 (es) |
CA (1) | CA2626976A1 (es) |
DE (1) | DE602006016314D1 (es) |
ES (1) | ES2349433T3 (es) |
HK (1) | HK1119680A1 (es) |
PE (1) | PE20070531A1 (es) |
TW (1) | TW200803847A (es) |
WO (1) | WO2007050721A2 (es) |
Families Citing this family (50)
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US7700603B2 (en) | 2003-12-15 | 2010-04-20 | Schering Corporation | Heterocyclic aspartyl protease inhibitors |
US20090221579A1 (en) * | 2004-10-15 | 2009-09-03 | Jeffrey Scott Albert | Substituted Amino-Compounds and Uses Thereof |
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WO2006138264A2 (en) | 2005-06-14 | 2006-12-28 | Schering Corporation | Aspartyl protease inhibitors |
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US7759354B2 (en) * | 2005-06-14 | 2010-07-20 | Schering Corporation | Bicyclic guanidine derivatives as asparyl protease inhibitors, compositions, and uses thereof |
CN101360720A (zh) * | 2005-11-15 | 2009-02-04 | 阿斯利康(瑞典)有限公司 | 新颖的2-氨基嘧啶酮衍生物及其用途 |
EP1951682A4 (en) * | 2005-11-15 | 2011-06-15 | Astrazeneca Ab | NEW 2-AMINOPYRIMIDONE OR 2-AMINOPYRIDINONE DERIVATIVES AND THEIR USE |
TW200734311A (en) * | 2005-11-21 | 2007-09-16 | Astrazeneca Ab | New compounds |
CN101360716A (zh) * | 2005-11-21 | 2009-02-04 | 阿斯利康(瑞典)有限公司 | 新颖的2-氨基-咪唑-4-酮化合物及其在制备用于治疗认知缺损、阿尔茨海默病、神经变性和痴呆的药物中的用途 |
AR058381A1 (es) * | 2005-12-19 | 2008-01-30 | Astrazeneca Ab | Compuestos derivados de 2-aminopiridin-4-onas y una composicion farmaceutica |
WO2007114771A1 (en) * | 2006-04-05 | 2007-10-11 | Astrazeneca Ab | 2-AMINOPYRIMIDIN-4-ONES AND THEIR USE FOR TREATING OR PREVENTING Aβ-RELATED PATHOLOGIES |
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TW200815447A (en) * | 2006-06-14 | 2008-04-01 | Astrazeneca Ab | Novel compounds IV |
US20080051420A1 (en) * | 2006-06-14 | 2008-02-28 | Astrazeneca Ab | New Compounds 317 |
TW200815349A (en) * | 2006-06-22 | 2008-04-01 | Astrazeneca Ab | New compounds |
TW200831484A (en) * | 2006-12-20 | 2008-08-01 | Astrazeneca Ab | New compounds |
TW200902499A (en) * | 2007-05-15 | 2009-01-16 | Astrazeneca Ab | New compounds |
TW200902503A (en) * | 2007-05-15 | 2009-01-16 | Astrazeneca Ab | New compounds |
WO2009032277A1 (en) | 2007-09-06 | 2009-03-12 | Schering Corporation | Gamma secretase modulators |
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CH523264A (de) | 1967-04-13 | 1972-05-31 | Ciba Geigy Ag | Verfahren zur Herstellung von 2,4 Benzdiazepinen |
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ATE489370T1 (de) | 2005-06-14 | 2010-12-15 | Schering Corp | Herstellung und verwendung von verbindungen als aspartylproteasehemmer |
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2006
- 2006-10-25 CA CA002626976A patent/CA2626976A1/en not_active Abandoned
- 2006-10-25 AR ARP060104660A patent/AR057983A1/es not_active Application Discontinuation
- 2006-10-25 ES ES06817385T patent/ES2349433T3/es active Active
- 2006-10-25 US US11/586,151 patent/US7763606B2/en active Active
- 2006-10-25 AT AT06817385T patent/ATE478070T1/de not_active IP Right Cessation
- 2006-10-25 JP JP2008537928A patent/JP2009513656A/ja not_active Ceased
- 2006-10-25 CN CNA2006800398031A patent/CN101296926A/zh active Pending
- 2006-10-25 PE PE2006001297A patent/PE20070531A1/es not_active Application Discontinuation
- 2006-10-25 EP EP06817385A patent/EP1940828B1/en active Active
- 2006-10-25 DE DE602006016314T patent/DE602006016314D1/de active Active
- 2006-10-25 WO PCT/US2006/041716 patent/WO2007050721A2/en active Application Filing
- 2006-10-26 TW TW095139559A patent/TW200803847A/zh unknown
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2008
- 2008-10-24 HK HK08111732.2A patent/HK1119680A1/xx not_active IP Right Cessation
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2010
- 2010-06-07 US US12/794,858 patent/US8012960B2/en active Active
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2011
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US20100247519A1 (en) | 2010-09-30 |
ES2349433T3 (es) | 2011-01-03 |
US20070099898A1 (en) | 2007-05-03 |
TW200803847A (en) | 2008-01-16 |
WO2007050721A2 (en) | 2007-05-03 |
CA2626976A1 (en) | 2007-05-03 |
US7763606B2 (en) | 2010-07-27 |
US8012960B2 (en) | 2011-09-06 |
WO2007050721A3 (en) | 2007-06-14 |
JP2009513656A (ja) | 2009-04-02 |
US20110280867A1 (en) | 2011-11-17 |
EP1940828B1 (en) | 2010-08-18 |
ATE478070T1 (de) | 2010-09-15 |
EP1940828A2 (en) | 2008-07-09 |
CN101296926A (zh) | 2008-10-29 |
HK1119680A1 (en) | 2009-03-13 |
PE20070531A1 (es) | 2007-07-13 |
DE602006016314D1 (de) | 2010-09-30 |
US8202854B2 (en) | 2012-06-19 |
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